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21 kD (Reducing)
50mM Tris-HCl，150mM NaCl，10mM EDTA，1mM DTT，50%(v/v) glycerol，（pH 8.0 @ 25℃）
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Store at -25 ~ -15℃ for 2 years
[1] Knott J A , Orr D C , Montgomery D S ,et al.The expression and purification of human rhinovirus protease 3C.[J].European Journal of Biochemistry, 1989, 182(3):547-55.
[2] Xu H , Wang Q , Zhang Z ,et al.A simplified method to remove fusion tags from a xylanase of Bacillus sp. HBP8 with HRV 3C protease[J].Enzyme and Microbial Technology, 2019, 123:15-20.
Recombinant human rhinovirus(HRV)3C protease is widely used in the purification and productions of proteins due to its good stability，high specificity，and enzymatic activity．3C protease is one of the non—structural proteins of HRV，and plays important roles in the life cycle of HRV．This protease specifically recognizes the sequence Leu-Glu-Val-Leu-Phe-Gln-Gly-Pro, and cleaves the peptide bond between Gln and Gly.
Storage Solution: 1U/μl 3C Protease50mM Tris-HCl，150mM NaCl，10mM EDTA，1mM DTT，50%(v/v) glycerol（pH 8.0 @ 25℃） 10*Reaction Buffer: 500mM Tris-HCl，1.5M NaCl，10mM EDTA，10mM DTT，（pH 7.5@ 25℃）
1. Combine 100 μg of fusion protein, 10 μl of 10*Reaction Bufferr and H20 (if necessary) to make a 100 μl total reaction volume. 2. Add 1 µl HRV 3C Protease 3. Incubate reaction at 5°C for 16 hour.
Please avoid repeated freeze-thaw cycles.
The results of 100μg substrate digestion separated under different quantity of 3C Protease, the reaction was incubated for 16h minutes at 5°C.
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